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7-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienoxy]chromen-2-one is a complex organic compound characterized by a chromenone core, which is a type of chromone with a double bond between carbons 2 and 3. The molecule features a 3,7,11-trimethyldodeca-2,6,10-trienoxy group attached to the 7-position of the chromenone, which consists of a dodecatrienyl moiety with three methyl groups at positions 3, 7, and 11. This specific arrangement of double bonds and methyl groups contributes to the compound's unique chemical properties and potential applications in various fields, such as pharmaceuticals or materials science. The compound's structure and functional groups may influence its reactivity, solubility, and interaction with other molecules, making it a subject of interest for further chemical and biological studies.

532-16-1

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532-16-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 532-16-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,3 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 532-16:
(5*5)+(4*3)+(3*2)+(2*1)+(1*6)=51
51 % 10 = 1
So 532-16-1 is a valid CAS Registry Number.
InChI:InChI=1/C24H30O3/c1-18(2)7-5-8-19(3)9-6-10-20(4)15-16-26-22-13-11-21-12-14-24(25)27-23(21)17-22/h7,9,11-15,17H,5-6,8,10,16H2,1-4H3/b19-9+,20-15+

532-16-1Downstream Products

532-16-1Relevant academic research and scientific papers

Synthesis of prenyloxy coumarin analogues and evaluation of their antioxidant, lipoxygenase (LOX) inhibitory and cytotoxic activity

Kavetsou, Eleni,Gkionis, Leonidas,Galani, Georgia,Gkolfinopoulou, Christina,Argyri, Letta,Pontiki, Eleni,Chroni, Angeliki,Hadjipavlou-Litina, Dimitra,Detsi, Anastasia

, p. 856 - 866 (2017)

Umbelliferone, 4-methyl-umbelliferone and their farnesyloxy and geranyloxy analogues were synthesized and evaluated for their antioxidant and soybean lipoxygenase inhibitory activity as well as their cytotoxicity against human neuroblastoma cell line SK-N-SH and human hepatoma cell line HepG2. Auraptene (3), followed by 4-methyl-auraptene (4) exhibit modest cytotoxity against the HepG2 cell line. The novel coumarin 6 combines a satisfactory lipoxygenase inhibitory activity with potent cytotoxicity against SK-N-SH cells, but not against HepG2 cells, thus it could be considered as a lead compound for the development of novel therapeutic agents against neuroblastoma.

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